61001-11-4 Usage
Chemical Class
The compound belongs to the class of imidazoisoquinoline derivatives.
Molecular Weight
The molecular weight of the compound is 269.72 g/mol.
Structure
The compound consists of an imidazoisoquinoline core structure with a 3-chlorophenyl substituent.
Pharmacological Activities
The compound has potential pharmacological activities and has been studied for its potential as a therapeutic agent for various conditions.
Research Interest
The compound's chemical structure and properties make it a subject of interest for further research and development in the fields of pharmaceuticals and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 61001-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,0 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61001-11:
(7*6)+(6*1)+(5*0)+(4*0)+(3*1)+(2*1)+(1*1)=54
54 % 10 = 4
So 61001-11-4 is a valid CAS Registry Number.
61001-11-4Relevant academic research and scientific papers
Copper-catalyzed c-h functionalization of pyridines and isoquinolines with vinyl azides: Synthesis of imidazo heterocycles
Donthiri, Ramachandra Reddy,Pappula, Venkatanarayana,Reddy, N. Naresh Kumar,Bairagi, Dipayan,Adimurthy, Subbarayappa
, p. 11277 - 11284 (2015/01/08)
Copper(I) iodide-catalyzed oxidative C(sp2)-H functionalization of pyridines and isoquinolines for the synthesis of imidazo[1,2-a]pyridines and 2-phenylimidazo[2,1-a]isoquinolines with vinyl azides under mild aerobic conditions is reported. Goo
Synthesis and pregnancy terminating activity of 2-arylimidazo[2,1-a]isoquinolines and isoindoles
Toja,Omodei Sale,Favara,Omodei-Sale,Cattaneo,Gallico,Galliani
, p. 1222 - 1226 (2007/10/02)
A series of 2-arylimidazo[2,1-a]isoquinolines (1-21), some 5,6-dihydro derivatives (22-28) and 2-phenyl-5H-imidazo[2,1-a]isoindole (29) were synthesized and tested for the pregnancy terminating activity in hamsters and rats. An efficient preparation of 2-
